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All product recalls associated with Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF).
Total Recalls
1000
Past Year
579
Class I (Serious)
91
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The firm's internal processes identified that certain lots may have an improperly sealed barrier that could potentially compromise sterility.
First layer of Uniform Scanning treatment fields is sometimes irradiated with incorrect Scanning Magnet setpoints resulting in the field size may be smaller than expected and the irradiated area may receive more dose than prescribed
Firm detected an increase in complaints related to fractured jaw tips of the Cardioblate Gemini-s.